NDC 63148-624 Guard

Ethyl Alcohol

NDC Product Code 63148-624

NDC 63148-624-10

Package Description: 59 mL in 1 BOTTLE, PLASTIC

NDC 63148-624-20

Package Description: 236 mL in 1 BOTTLE, PLASTIC

NDC 63148-624-30

Package Description: 443 mL in 1 BOTTLE, PLASTIC

NDC 63148-624-40

Package Description: 946 mL in 1 BOTTLE, PLASTIC

NDC 63148-624-50

Package Description: 1182 mL in 1 BOTTLE, PLASTIC

NDC 63148-624-60

Package Description: 1892 mL in 1 BOTTLE, PLASTIC

NDC 63148-624-70

Package Description: 3785 mL in 1 BOTTLE, PLASTIC

NDC Product Information

Guard with NDC 63148-624 is a a human over the counter drug product labeled by Apollo Health And Beauty Care Inc. The generic name of Guard is ethyl alcohol. The product's dosage form is gel and is administered via topical form.

Labeler Name: Apollo Health And Beauty Care Inc

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Guard Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ALCOHOL 750 mg/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Apollo Health And Beauty Care Inc
Labeler Code: 63148
FDA Application Number: part333E What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 11-23-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Guard Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Ethyl Alcohol (75%)




For Personal hand hygiene to help the spread of bacteria and can be used in place of hand washing if soap and water are not available.


  • For External use onlyFlammableKeep away from source of heat or fire.

When Using This Product

Avoid contact with eyes. If contact occurs, rinse thoroughly with water. Do not Inhale.

Do Not Use

  • On children less than 2 months of ageon open skin woundson broken or damaged skin

Stop Use And Ask A Doctor

If Irritation or redness develops and lasts.

Keep Out Of Reach Of Children

In case of accidental ingestion, get medical help or contact a Poison Control Centre immediately


  • For occasional and personal useRub thoroughly into hands for at least 30 seconds. Allow to dryChildren under 6 years should be supervised when using this product

Other Information

  • Store at a temperature below 1100F (430C)May discolor certain fabrics or surfaces

Inactive Ingredients

Water (Aqua), PEG-6, Fragrance (Parfum), Isopropyl Alcohol, Glycerin, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, AMP-Acrylates/Vinyl Isodecanate Crosspolymer

* Please review the disclaimer below.